SITU GROWN SiC COATINGS ON CARBON MATERIALS

ABSTRACT

A method of forming a β-SiC material or coating by mixing SiO 2  with carbon and heating the mixture in vacuum wherein the carbon is oxidized to CO gas and reduces the SiO 2  to SiO gas and reacting a carbon material with the SiO gas at a temperature in the range of 1300 to 1600° C. resulting in a SiC material or a SiC coating on a substrate. Also disclosed is the related SiC material or coating prepared by this method.

CROSS-REFERENCE TO RELATED APPLICATIONS

This Application claims the benefit of U.S. Provisional Application61/477,668 filed on Apr. 21, 2011, the entire contents of which areincorporated herein by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates generally to SiC coatings and morespecifically to SiC coatings on carbon materials.

2. Description of the Prior Art

SiC is a hard, strong, chemically resistant material that is thermallyand electrically conductive. Due to its covalent bonding, it is verydifficult to densify without the use of additives that compromise itsmaterial properties. However, in many cases a monolithic material is notneeded. SiC can be deposited as a coating by techniques such as chemicalvapor deposition (CVD), plasma enhanced CVD, and direct chemicalreaction between carbon and molten silicon. SiC coatings are used toprotect a weaker or less resistant material by isolating it from theenvironment. The protection can be in the form of mechanical protectionsuch as wear or abrasion resistance, or chemical protection in corrosiveor reactive environments. Examples of mechanical protection are wearresistant coatings on bearings and wear plates. Examples of chemicalprotection are coated filters for molten metals and coatings for thechemical industry. An example of a combination of wear resistance andchemical resistance where SiC coating are used is in gas turbineengines.

CVD of SiC requires specialized equipment that can hold temperatures of2000° C. at a pressure of 0.5 Torr+/−0.001 for up to 10 days. The growthprocess is relatively slow and expensive. The gasses used aremethylsilane and trimethylsilane which are extremely flammable andconsidered hazardous.

The direct chemical method infiltrates carbon fleece with molten siliconat 1700° C. The carbon and Si is placed on the material to be coated andheated to 700° C. to bond. The substrate and carbon and silicon mix isheated to 1700° C. to react the Si and C to make SiC. The reaction isgenerally not complete and is composed of SiC and free Si. Since thereaction is a liquid phase reaction, the impurities are not volatilizedas they are in a vapor phase reaction and result in a coating that isdependent on the purity of the silicon.

BRIEF SUMMARY OF THE INVENTION

The aforementioned problems are overcome in the present invention whichprovides a method of forming a β-SiC material or coating by mixing SiO₂with carbon and heating the mixture in vacuum wherein the carbon isoxidized to CO gas and reduces the SiO₂ to SiO gas and reacting a carbonmaterial with the SiO gas at a temperature in the range of 1300 to 1600°C. resulting in a SiC material or a SiC coating on a substrate. Alsodisclosed is the related SiC material or coating prepared by thismethod.

The present invention provides a technique to coat substrates with SiCthat can be operated as low as 1300° C., which is a much lowertemperature than previous techniques: CVD of SiC operates at 2000° C.while the direst chemical method operates at 1700° C. The lowertemperature opens up the coating technique to many non-refractorymaterials and even some commercially important metals such as steel andtitanium.

The present invention also provides a technique that uses inexpensiveraw materials that are not hazardous. CVD uses expensive liquids andgasses that are hazardous. This would decrease the cost of coating SiCnot only due to the lower raw material cost, but also because handlingof flammable and toxic precursors and waste material is no longernecessary.

The present invention further provides a technique that uses simplevacuum furnaces and reaction vessels unlike CVD where specializedequipment is needed.

These and other features and advantages of the invention, as well as theinvention itself, will become better understood by reference to thefollowing detailed description, appended claims, and accompanyingdrawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an uncoated vitreous carbon disk (left) and an SiC coatedvitreous carbon disk (right).

FIG. 2 is an XRD pattern of an as-received vitreous carbon disk (bottom)and a vitreous carbon disk that was run at 1600° C. for 4 hours showingthe formation of a β-SiC coating (top) C-vitreous carbon, β- β-SiC.

FIG. 3 shows an uncoated crucible (left) and an SiC-coated crucible(right).

DETAILED DESCRIPTION OF THE INVENTION

The present invention pertains to forming β-SiC on a carbon containingsubstrate. The SiC can be in the form of a coating or can completelyreplace the carbon material with β-SiC. It is also possible to coat amaterial not containing carbon by first coating said material withcarbon and then reacting the carbon coating to form β-SiC.

The β-SiC can be deposited on a carbon substrate by reacting said carbonsubstrate with SiO gas. A carbon substrate is defined as all materialsthat are made up of carbon such as, but not limited to graphite,vitreous carbon, amorphous carbon, and diamond. The SiO directly reactsat temperatures of 1300-1600° C. with the carbon to form a coating or ifthe material is sufficiently thin (<50 microns) the entirety of thematerial can be converted to β-SiC.

The SiO gas is formed by mixing SiO₂ with carbon and heating in vacuum.The carbon is oxidized to CO gas and reduces the SiO₂ to SiO gas whichflows over the carbon substrate and forms SiC. SiO₂ includes but is notlimited to powder, alkoxide precursors, crystalline or glassymorphologies. Carbon includes any material that can supply carbon to thereaction such as graphite, vitreous carbon, activated carbon, carbonblack, and carbon containing organic compounds such as sugar, fructose,and sucrose.

The material can be heated in a sintering furnace capable of operatingin vacuum. The reaction vessel can be as simple as a lidded cruciblewith the part to be coated suspended inside the crucible. A more complexvessel would have a reaction zone for the SiO₂ and C and a fixture forthe substrate to be coated. The vessel is loaded with the SiO₂+C chargeand the substrate. The vessel is sealed and placed in the furnace. Thefurnace is ramped at 5° C./minute to the operating temperature and held.The result will be a SiC coated substrate.

Alternatively the substrate can be a porous carbon material. In thiscase the entirety of the carbon may be converted to SiC due to thethinness of the carbon structural units in the porous material.

New designs of the reaction vessel can be envisioned to coat multiplesamples at once. It may also be possible to form the SiO gas at onetemperature while the material to be coated is at a much lowertemperature. It may be possible to form the SiO gas using otherreactants that do not involve the reduction of SiO₂ by carbon.

EXAMPLE 1

SiO₂ powder and activated carbon are mixed with a mortar and pestle. Themixture is placed in a vitreous carbon reaction vessel. A vitreouscarbon disk is placed in the vessel. The vessel is placed in a graphitevacuum furnace and heated to 1600° C. at 5° C./min and held for 4 hours.FIG. 1 shows a photograph of the disk before and after coating with SiC.FIG. 2 is an X-ray diffraction pattern of the vitreous carbon diskbefore and after coating.

EXAMPLE 2

Tetraethylorthosilicate (TEOS) which is an alkoxide precursor for SiO₂is mixed with dissolved sugar and dried. The dried mixture is placed ina vitreous carbon crucible having a large height to diameter ratio. Thecrucible is caped, placed in a vacuum furnace and heated at 5° C./minuteto 1600° C. for 10 hours. FIG. 3 shows an uncoated crucible and aSiC-coated crucible.

EXAMPLE 3

This example is the same process as either example 1 or 2 with theexception that a porous carbon material is placed in the reactionvessel. The result is a SiC porous material.

EXAMPLE 4

This example uses an alternative host, in this case Al₂O₃, although itcould be any other substrate, which was coated with a carbon coating.The surface was then reacted in a similar manner to example 1. Thisconverted the carbon coating to SiC.

EXAMPLE 5

This example uses an alternative host, in this case stainless steel,which was coated with a carbon coating. The surface was then reacted ina similar manner to example 1. This converted the carbon coating to SiC.

The above descriptions are those of the preferred embodiments of theinvention. Various modifications and variations are possible in light ofthe above teachings without departing from the spirit and broaderaspects of the invention. It is therefore to be understood that theclaimed invention may be practiced otherwise than as specificallydescribed. Any references to claim elements in the singular, forexample, using the articles “a,” “an,” “the,” or “said,” are not to beconstrued as limiting the element to the singular.

1. A method of forming β-SiC on a carbon substrate comprising: mixingSiO₂ with carbon and heating the mixture in vacuum wherein the carbon isoxidized to CO gas and reduces the SiO₂ to SiO gas; and reacting thecarbon substrate with the SiO gas at a temperature in the range of 1300to 1600° C. resulting in a SiC coating on the carbon substrate.
 2. Themethod of claim 1, wherein the carbon substrate comprises graphite,vitreous carbon, amorphous carbon, diamond, or any combination thereof.3. The method of claim 1, wherein SiO₂ is a powder, an alkoxideprecursor, a crystalline or glassy morphology, or any combinationthereof.
 4. The method of claim 1, wherein the carbon mixed with theSiO₂ comprises graphite, vitreous carbon, activated carbon, carbonblack, carbon containing organic compounds, or any combination thereof.5. The method of claim 1, wherein the carbon substrate can be preparedby coating a substrate not containing carbon with carbon to form acarbon coating on the substrate.
 6. The method of claim 1, wherein thecarbon substrate is Al₂O₃ with a carbon coating or stainless steel witha carbon coating.
 7. A method of forming β-SiC comprising: mixing SiO₂with carbon and heating the mixture in vacuum wherein the carbon isoxidized to CO gas and reduces the SiO₂ to SiO gas; and reacting acarbon material with the SiO gas at a temperature in the range of 1300to 1600° C. wherein the carbon material converts to SiC.
 8. The methodof claim 7, wherein the thickness of the carbon material is 50 micronsor less.
 9. The method of claim 7, wherein the carbon material isporous.
 10. The method of claim 7, wherein the carbon material comprisesgraphite, vitreous carbon, amorphous carbon, diamond, or any combinationthereof.
 11. The method of claim 7, wherein SiO₂ is a powder, analkoxide precursor, a crystalline or glassy morphology, or anycombination thereof.
 12. The method of claim 7, wherein the carbon mixedwith the SiO₂ comprises graphite, vitreous carbon, activated carbon,carbon black, carbon containing organic compounds, or any combinationthereof.
 13. A β-SiC material or coating formed by the methodcomprising: mixing SiO₂ with carbon and heating the mixture in vacuumwherein the carbon is oxidized to CO gas and reduces the SiO₂ to SiOgas; and reacting a carbon material with the SiO gas at a temperature inthe range of 1300 to 1600° C. resulting in a SiC or an SiC coating onthe carbon material.
 14. The method of claim 13, wherein the carbonmaterial comprises graphite, vitreous carbon, amorphous carbon, diamond,or any combination thereof.
 15. The method of claim 13, wherein SiO₂ isa powder, an alkoxide precursor, a crystalline or glassy morphology, orany combination thereof.
 16. The method of claim 13, wherein the carbonmixed with the SiO₂ comprises graphite, vitreous carbon, activatedcarbon, carbon black, carbon containing organic compounds, or anycombination thereof.
 17. The method of claim 13, wherein the carbonmaterial can be prepared by coating a substrate not containing carbonwith carbon to form a substrate with a carbon coating.
 18. The method ofclaim 13, wherein the carbon material is Al₂O₃ with a carbon coating orstainless steel with a carbon coating.
 19. The method of claim 13,wherein the thickness of the carbon material is 50 microns or less. 20.The method of claim 13, wherein the carbon material is porous.